Ong Wei-Yi, Herr Deron R, Farooqui Tahira, Ling Eng-Ang, Farooqui Akhlaq A
a 1 National University of Singapore, Department of Anatomy , Singapore 119260, Singapore +65 6516 3662 ; +65 6778 7643 ;
b 2 National University of Singapore, Neurobiology and Ageing Research Programme , Singapore 119260, Singapore.
Expert Opin Ther Targets. 2015;19(12):1725-42. doi: 10.1517/14728222.2015.1071794. Epub 2015 Aug 4.
Sphingomyelinases, which catalyze the hydrolysis of sphingomyelin to ceramide and phosphorylcholine, are abundant in the brain. These enzymes are a major, rapid source of ceramide production not only during physiological responses to receptor stimulation, but also in neurological disorders.
We covered an introduction to sphingomyelinases and its enzymatic product ceramide, in membrane domains or lipid rafts and the nucleus; followed by crosstalk between sphingomyelinase and cytosolic phospholipase A2 (cPLA2) catalysed products including arachidonic acid, functions of acid sphingomyelinase (aSMase) and neutral sphingomyelinase (N-SMase) in neurons, neuronal progenitor cells, glial cells, and brain endothelial cells; alterations in acid and N-SMases in Niemann Pick Disease Type A, major depression, Alzheimer's disease, cerebral ischemia, and pain; and recent developments in identification of inhibitors to sphingomyelinases. As literature search methodology, we did key word searches using Pubmed.
More research needs to be carried out to develop pharmacological agents that act on sphingomyelinases, for the prevention or treatment of neurological disorders.
鞘磷脂酶可催化鞘磷脂水解生成神经酰胺和磷酸胆碱,在大脑中含量丰富。这些酶不仅是生理条件下受体刺激反应过程中神经酰胺产生的主要快速来源,也是神经疾病中神经酰胺产生的主要快速来源。
我们介绍了鞘磷脂酶及其酶促产物神经酰胺,包括其在膜结构域或脂筏以及细胞核中的情况;接着阐述了鞘磷脂酶与胞质磷脂酶A2(cPLA2)催化产物(包括花生四烯酸)之间的相互作用,酸性鞘磷脂酶(aSMase)和中性鞘磷脂酶(N-SMase)在神经元、神经祖细胞、神经胶质细胞和脑内皮细胞中的功能;在A型尼曼匹克病、重度抑郁症、阿尔茨海默病、脑缺血和疼痛中酸性和N-SMase的变化;以及鞘磷脂酶抑制剂鉴定方面的最新进展。作为文献检索方法,我们使用PubMed进行关键词搜索。
需要开展更多研究以开发作用于鞘磷脂酶的药物制剂,用于预防或治疗神经疾病。